A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737807



Internal ID161473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146955606..146961606hg38UCSC Ensembl
chrX:146037124..146043124hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737807
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0595664


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